International safety notice
Ανάκληση παρτίδας RN19 του οδηγού νεφρικής αρτηρίας Destination Για να δείτε την απόφαση, πατήστε εδώ
Greece / EOF · GRC · Dec 10, 2015
Key facts
| Title | Ανάκληση παρτίδας RN19 του οδηγού νεφρικής αρτηρίας Destination Για να δείτε την απόφαση, πατήστε εδώ |
|---|---|
| Regulator | Greece / EOF |
| Country | GRC |
| Brand | Terumo Europe N.V. |
| Manufacturer | Μ.Σ. Ιακωβίδης Ελλάς Α.Ε. |
| Models | 85084, 130648, 84221, Ν.1316, 2040435, “RSR01”, 26-11-2015, 01-12-2015, 6549500 |
| Event type | Recall, Safety Notice |
| Date | Dec 10, 2015 |
| Regulator page | eof.gr |
At a glance
- Yes Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1